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41
LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation
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Artigo
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LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation

Bohlega, Saeed A. ; Alfawaz, Sarah ; Abou-Al-Shaar, Hussam ; Al-Hindi, Hindi N. ; Murad, Hatem N. ; Bohlega, Mohamed S. ; Meyer, Brian F. ; Monies, Dorota

Acta myologica, 2018-09, Vol.37 (3), p.221-226 [Periódico revisado por pares]

Pacini Editore srl

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42
Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)
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Artigo
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Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)

Abusrair, Ali ; Bohlega, Saeed

Neurology, 2019-04, Vol.92 (15_supplement) [Periódico revisado por pares]

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43
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3
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Artigo
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SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3

Alazami, Anas M ; Alzahrani, Fatema ; Bohlega, Saeed ; Alkuraya, Fowzan S

Neurology, 2014-05, Vol.82 (18), p.1665-1666 [Periódico revisado por pares]

United States: American Academy of Neurology

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44
Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience
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Artigo
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Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience

Bohlega, Saeed ; Abou Al-Shaar, Hussam ; Alkhairallah, Thamer ; Al-Ajlan, Fahad ; Hasan, Nael ; Alkahtani, Khalid

European neurology, 2015-01, Vol.74 (5-6), p.227-236 [Periódico revisado por pares]

Basel, Switzerland: S. Karger AG

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45
Mutations in NHLRC1 cause progressive myoclonus epilepsy
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Artigo
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Mutations in NHLRC1 cause progressive myoclonus epilepsy

Minassian, Berge A ; Scherer, Stephen W ; Chan, Elayne M ; Young, Edwin J ; Ianzano, Leonarda ; Munteanu, Iulia ; Zhao, Xiaochu ; Christopoulos, Constantine C ; Avanzini, Giuliano ; Elia, Maurizio ; Ackerley, Cameron A ; Jovic, Nebojsa J ; Bohlega, Saeed ; Andermann, Eva ; Rouleau, Guy A ; Delgado-Escueta, Antonio V

Nature genetics, 2003-10, Vol.35 (2), p.125-127 [Periódico revisado por pares]

London: Nature Publishing Group

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46
Economic Evaluation of Cladribine Tablets in Patients With High Disease Activity–Relapsing-Remitting Multiple Sclerosis in the Kingdom of Saudi Arabia
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Artigo
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Economic Evaluation of Cladribine Tablets in Patients With High Disease Activity–Relapsing-Remitting Multiple Sclerosis in the Kingdom of Saudi Arabia

Bohlega, Saeed ; Elboghdady, Ahmed ; Al-Johani, Awatef ; Mahajan, Koshu ; Mughari, Majdoline Khalil ; Al-Saqa’aby, Mai ; Mohamed, Omneya ; Alarieh, Rola ; Al Malik, Yaser

Value in health regional issues, 2021-09, Vol.25, p.189-195 [Periódico revisado por pares]

United States: Elsevier Inc

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47
Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group
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Artigo
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Diagnosis and treatment of late-onset Pompe disease in the Middle East and North Africa region: consensus recommendations from an expert group

Al Jasmi, Fatma ; Al Jumah, Mohammed ; Alqarni, Fatimah ; Al-Sanna'a, Nouriya ; Al-Sharif, Fawziah ; Bohlega, Saeed ; Cupler, Edward J ; Fathalla, Waseem ; Hamdan, Mohamed A ; Makhseed, Nawal ; Nafissi, Shahriar ; Nilipour, Yalda ; Selim, Laila ; Shembesh, Nuri ; Sunbul, Rawda ; Tonekaboni, Seyed Hassan

BMC neurology, 2015-10, Vol.15 (1), p.205-205, Article 205 [Periódico revisado por pares]

England: BioMed Central Ltd

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48
Functional clinical outcomes in multiple sclerosis: Current status and future prospects
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Artigo
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Functional clinical outcomes in multiple sclerosis: Current status and future prospects

Karabudak, Rana ; Dahdaleh, Maurice ; Aljumah, Mohammed ; Alroughani, Raed ; Alsharoqi, I. Ahmed ; AlTahan, Abdulrahman M ; Bohlega, Saeed A ; Daif, Abdulkader ; Deleu, Dirk ; Amous, Amer ; Inshasi, Jihad S ; Rieckmann, Peter ; Sahraian, Mohammed A ; Yamout, Bassem I

Multiple sclerosis and related disorders, 2015-05, Vol.4 (3), p.192-201

Netherlands: Elsevier B.V

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49
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies
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Artigo
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A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies

Monies, Dorota ; Alhindi, Hindi N ; Almuhaizea, Mohamed A ; Abouelhoda, Mohamed ; Alazami, Anas M ; Goljan, Ewa ; Alyounes, Banan ; Jaroudi, Dyala ; AlIssa, Abdulelah ; Alabdulrahman, Khalid ; Subhani, Shazia ; El-Kalioby, Mohamed ; Faquih, Tariq ; Wakil, Salma M ; Altassan, Nada A ; Meyer, Brian F ; Bohlega, Saeed

Human genomics, 2016-09, Vol.10 (1), p.32-32, Article 32 [Periódico revisado por pares]

England: BioMed Central

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50
In silico analysis of influence of the missense mutation P629S on the molecular interaction and 3D properties of PIK3R5
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Artigo
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In silico analysis of influence of the missense mutation P629S on the molecular interaction and 3D properties of PIK3R5

Shinwari, Jameela ; Tahir, Asma I. ; Bohlega, Saeed ; AlTassan, Nada

Advances in biological chemistry, 2013, Vol.3 (4), p.408-417

Scientific Research Publishing, Inc

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